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西妥昔单抗偶联羟基磷灰石锆纳米颗粒作为纳米载体在肺癌X射线动态治疗和基于镥的放射免疫治疗中作为放射增敏剂的双重潜力。

Dual Potential of Cetuximab Conjugated Hydroxyapatite Zirconium Nanoparticle as Nanocarrier for Radioenhancer in X-Ray Dynamic Therapy and Lu-based Radioimmunotherapy of Lung Cancer.

作者信息

Kurniawan Ahmad, Mahendra Isa, Rizaludin Asep, Utama Marhendra Satria, Lesmana Ronny, Ayuningtyas Fitria Dwi, Dewanti Maria Rosa, Syarif Dani Gustaman, Febrian Muhamad Basit

机构信息

Research Center for Radioisotope, Radiopharmaceuticals and Biodosimetry Technology, National Research and Innovation Agency, Serpong, Indonesia.

Department of Radiology, Faculty of Medicine, Universitas Padjadjaran/Dr. Hasan Sadikin General Hospital, Bandung, Indonesia.

出版信息

Nanotheranostics. 2025 Mar 3;9(1):82-94. doi: 10.7150/ntno.101699. eCollection 2025.

DOI:10.7150/ntno.101699
PMID:40078313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11898717/
Abstract

This study aimed to synthesize cetuximab (CTX) conjugated hydroxyapatite zirconium (HApZr-CTX) as a nanocarrier for active delivery of photosensitizer and therapeutic radionuclide. The system enabled targeted radioenhancer in X-ray dynamic therapy and radioimmunotherapy for lung cancer. The results showed that HApZr-CTX had the main characteristics of hydroxyapatite crystal in X-ray powder diffraction (XRD), with particle size twice bigger, according to DLS-PSA and TEM measurements. Cellular ROS generation was elevated almost three times in A549 cells after being treated using 125 µg/mL HApZr-CTX and irradiated with 5 Gy of X-ray photon compared to untreated cells. The viability of the treated lung cancer cell line decreased after exposure to external radiation. Moreover, as a radioimmunotherapy candidate, Lu was successfully loaded into HApZr-CTX nanocarrier and internalized in A549 more than half of the given dose after 0.5 h incubation. [Lu]Lu-HApZr-CTX was primarily accumulated in the lung organs of healthy mice one-hour post-injection. In conclusion, HApZr-CTX nanoparticles have the potential to be used as a radioenhancer in X-ray dynamic therapy and radioimmunotherapy for lung cancer therapy.

摘要

本研究旨在合成西妥昔单抗(CTX)偶联的羟基磷灰石锆(HApZr - CTX)作为纳米载体,用于主动递送光敏剂和治疗性放射性核素。该系统可在肺癌的X射线动态治疗和放射免疫治疗中实现靶向放射增强。结果表明,根据动态光散射 - 颗粒大小分析仪(DLS - PSA)和透射电子显微镜(TEM)测量,HApZr - CTX在X射线粉末衍射(XRD)中具有羟基磷灰石晶体的主要特征,粒径大两倍。与未处理的细胞相比,使用125μg/mL HApZr - CTX处理并接受5 Gy X射线光子照射后,A549细胞中的细胞活性氧生成增加了近三倍。经外部辐射后,处理过的肺癌细胞系的活力下降。此外,作为放射免疫治疗候选物,镥(Lu)成功加载到HApZr - CTX纳米载体中,孵育0.5小时后,超过一半的给药剂量内化于A549细胞中。注射后一小时,[镥 - 177]Lu - HApZr - CTX主要积聚在健康小鼠的肺部器官。总之,HApZr - CTX纳米颗粒有潜力在肺癌治疗的X射线动态治疗和放射免疫治疗中用作放射增强剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8954/11898717/ca122aecd442/ntnov09p0082g008.jpg
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本文引用的文献

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